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Merck

L7914

Lipoprotein, low density from human plasma

≥95% (SDS-PAGE), solution

Sinónimos:

β-Lipoprotein, LDL, Low density lipoprotein

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Número CAS:
UNSPSC Code:
12352211
NACRES:
NA.25
MDL number:
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Nombre del producto

Lipoprotein, low density from human plasma, ≥95% (SDS-PAGE), solution

biological source

human plasma

assay

≥95% (SDS-PAGE)

form

solution

UniProt accession no.

functional group

ester
phospholipid

shipped in

wet ice

storage temp.

2-8°C

Quality Level

Gene Information

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Application

Lipoprotein, low density from human plasma has been used:
  • as an additive in cholesterol-free RPMI media
  • as a component in buffer to perform an assay for measuring lipid peroxidation
  • to stimulate hepatic macrophages
  • as a plasma protein to determine pazopanib unbound fraction (fu%) by equilibrium dialysis

Biochem/physiol Actions

LDL and HDL transport both dietary and endogenous cholesterol in the plasma. LDL is the main transporter of cholesterol and cholesteryl esters and makes up more than half of the total lipoprotein in plasma. LDL is absorbed by the liver and other tissues via receptor mediated endocytosis. The cytoplasmic domain of the LDL receptor facilitates the formation of coated pits; receptor-rich regions of the membrane. The ligand binding domain of the receptor recognizes apo-B100 on LDL, resulting in the formation of a clathrin-coated vesicle. ATP-dependent proton pumps lower the pH inside the vesicle resulting dissociation of LDL from its receptor. After loss of the clathrin coat the vesicles fuse with lysozomes, resulting in peptide and cholesteryl ester enzymatic hydrolysis. The LDL receptor can be recycled to the cell membrane. Insulin, tri-iodothyronine and dexamethasome have shown to be involved with the regulation of LDL receptor mediated uptake.

Disclaimer

Freezing of lipoprotein solutions may cause structural or compositional changes.
RESEARCH USE ONLY. This product is regulated in France when intended to be used for scientific purposes, including for import and export activities (Article L 1211-1 paragraph 2 of the Public Health Code). The purchaser (i.e. enduser) is required to obtain an import authorization from the France Ministry of Research referred in the Article L1245-5-1 II. of Public Health Code. By ordering this product, you are confirming that you have obtained the proper import authorization.

General description

Low density lipoproteins are smaller than VLDL and IDL (26 nm) (MW approximately 3.5 million) and more dense (~1.04). The protein component of LDL is apolipoprotein B100. LDL contains 20-22% protein, 10-15% triglycerides, 20-28% phospholipids, 37-48% cholesteryl esters and 8-10% cholesterol.

Physical form

Solution in 150 mM NaCl and 0.01% EDTA, pH 7.4

Clase de almacenamiento

10 - Combustible liquids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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Leanne Satchell et al.
Biochemistry, 51(18), 3767-3775 (2012-04-13)
Low-density lipoprotein (LDL) has recently been shown to be oxidized by iron within the lysosomes of macrophages, and this is a novel potential mechanism for LDL oxidation in atherosclerosis. Our aim was to characterize the chemical and physical changes induced
S P Zhao et al.
Clinica chimica acta; international journal of clinical chemistry, 203(2-3), 109-117 (1991-12-16)
After 15 weeks of simvastatin therapy (20 mg/day), low density lipoprotein particle size in sera of 16 patients with type IIb hyperlipoproteinemia increased significantly from 233 +/- 5.0 A to 237 +/- 7.0 A (P less than 0.05), analyzed by
L L Rudel et al.
The Biochemical journal, 139(1), 89-95 (1974-04-01)
1. A simple method for isolation of individual human plasma lipoprotein classes is presented. In this technique, lipoproteins are removed from plasma at d1.225 by ultracentrifugation, after which they are separated and purified by agarose-column chromatography. 2. Three major classes
Ezetimibe suppresses development of liver tumors by inhibiting angiogenesis in mice fed a high-fat diet
Miura K, et al.
Cancer Science, 110(2), 771-771 (2019)
Determination of unbound fraction of pazopanib in vitro and in cancer patients reveals albumin as the main binding site
Imbs DC, et al.
Investigational New Drugs, 34(1), 41-48 (2016)

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